166 results on '"Hölttä T"'
Search Results
2. Terrestrial laser scanning intensity captures diurnal variation in leaf water potential
- Author
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Junttila, S., Hölttä, T., Puttonen, E., Katoh, M., Vastaranta, M., Kaartinen, H., Holopainen, M., and Hyyppä, H.
- Published
- 2021
- Full Text
- View/download PDF
3. A mechanistic model of winter stem diameter dynamics reveals the time constant of diameter changes and the elastic modulus across tissues and species
- Author
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Lindfors, L., Atherton, J., Riikonen, A., and Hölttä, T.
- Published
- 2019
- Full Text
- View/download PDF
4. Bursts of CO₂ released during freezing offer a new perspective on avoidance of winter embolism in trees
- Author
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Lintunen, A., Lindfors, L., Kolari, P., Juurola, E., Nikinmaa, E., and Hölttä, T.
- Published
- 2014
5. Global transpiration data from sap flow measurements: The SAPFLUXNET database
- Author
-
Ministerio de Ciencia e Innovación (España), Agència de Gestió d'Ajuts Universitaris i de Recerca, Poyatos, R [0000-0003-0521-2523], Granda, V [0000-0002-0469-1991], Flo, V [0000-0003-1908-4577], Adams, MA [0000-0002-8154-0097], Adorjan, B [0000-0002-5482-2515], Aidar, MPM [0000-0001-5728-6749], Alvarado-Barrientos, MS [0000-0003-0098-0806], Anderson-Teixeira, KJ [0000-0001-7585-712X], Arain, MA [0000-0002-1433-5173], Aranda, I [0000-0001-9086-7940], Asbjornsen, H [000-0001-8126-3328], Oishi, AC [0000-0001-5064-4080], Oliveira RS [0000-0002-6392-2526], Oren, R [0000-0002-5654-1733], Ourcival,JM [0000-0002-3557-3496], Paljakka, T [0000-0002-3674-4904], Perez-Priego, O [0000-0002-3138-3177], Peri, PL [0000-0002-5398-4408], Peters, RL [0000-0002-7441-1297], Pfautsch, S [0000-0002-4390-4195], Pockman, WT [0000-0002-3286-0457], Baxter, R [0000-0002-7504-6797], Preisler, Y [0000-0001-5861-8362], Rocha, H [0000-0002-5981-4469], Röll, A [0000-0001-9457-4459], Rosado, BHP [0000-0002-8924-8672], Rowland, L [0000-0002-0774-3216], Rubtsov, A [0000-0002-9663-4344], Sabaté, S [0000-0003-1854-0761], Salmon, Y [0000-0003-4433-4021], Salomón, RL [0000-0003-2674-1731], Sánchez-Costa, E [0000-0001-6799-9611], Beamesderfer, E [0000-0002-7513-7349], Schäfer, K [0000-0001-9452-3619], Schuldt, B [0000-0003-4738-5289], Shashkin, A [0000-0001-9925-5019], Stahl, C [0000-0001-5411-1169], Stojanović, M [0000-0003-4918-8668], Sun, G [0000-0002-0159-1370], Szatniewska, J [0000-0003-3027-9965], Tatarinov, F [0000-0002-8338-6070], Tesar, M [0000-0002-5647-8498], Thomas, FM [0000-0001-6377-719X], Berveiller, D [0000-0001-7461-6420], Tor-ngern, P [0000-0001-7363-4926], Urban, J [0000-0003-1730-947X], Van der Tol, C [0000-0002-2484-8191], Van Meerveld [0000-0002-7547-3270], Varlagin, A [0000-0002-2549-5236], Werner, C [0000-0002-7676-9057], Wieser, G [0000-0002-7575-5657], Wingate, W [0000-0003-1921-1556], Wullschleger, S [0000-0002-9869-0446], Koong, Y [0000-0002-8630-3031], Blakely, B [0000-0001-9923-0794], Zweifel, R [0000-0001-9438-0582], Steppe, K [0000-0001-6252-0704], Mencuccini, M [0000-0003-0840-1477], Martínez-Vilalta, J [0000-0002-2332-7298], Boggs, J [0000-0003-4826-1843], Bohrer, G [0000-0002-9209-9540], Bolstad, P [0000-0002-1829-8859], Bonal, D [0000-0001-9602-8603], Bracho, R [0000-0002-8015-9796], Brodeur, J [0000-0001-7118-8360], Casanoves, F [0000-0001-8765-9382], Chave, J [0000-0002-7766-1347], Chen, H [0000-0001-7619-3425], Cisneros, C [0000-0001-9661-4581], Clark, K [0000-0003-0534-9677], Cremonese, E [0000-0002-6708-8532], Dang, H [0000-0003-4428-3834], David, J [0000-0001-6994-1085], David, T [0000-0003-1473-899X], Delpierre, D [0000-0003-0906-9402], Desai, AR [0000-0002-5226-6041], Do, FC [0000-0002-2852-627X], Dohnal, M [0000-0003-1769-4750], Domec, JC [0000-0003-0478-2559], Dzikiti, S [0000-0002-1892-4143], Edgar, C [0000-0002-7026-8358], Eichstaedt, R [0000-0002-4905-7994], El-Madany, T [0000-0002-0726-7141], Elbers, J [0000-0002-0631-3505], Eller, CB [0000-0002-7795-2574], Euskirchen, E [0000-0002-0848-4295], Ewers, B [0000-0001-6647-7475], Fonti, P [0000-0002-7070-3292], Forner, A [0000-0002-7123-6403], Forrester, D [0000-0003-2732-5692], Freitas, HC [0000-0002-4861-1164], Galvagno, M [0000-0002-0827-487X], Garcia-Tejera, O [0000-0001-7726-8118], Ghimire, CP [0000-0002-3715-6311], Gimeno, TE [0000-0002-1707-9291], Granier, A [0000-0002-4174-2487], Griebel, A [0000-0002-4476-8279], Guangyu, Y [0000-0003-3242-5348], Gush, MB [0000-0003-1328-9862], Hanson, PJ [0000-0001-7293-3561], Hasselquist, N [0000-0003-2777-0163], Heinrich, I [0000-0001-5800-6999], Hernandez-Santana, V [0000-0001-9018-8622], Herrmann, V [0000-0002-4519-481X], Hölttä, T [0000-0001-7677-7156], Holwerda, F [0000-0003-4125-1765], Ayutthaya, SIN [0000-0002-5354-1527], Jochheim,H [0000-0001-8047-4553], Joly, CA [0000-0002-7945-2805], Kim, HS [0000-0002-3440-6071], Klemedtsson, L [0000-0002-1122-0717], Kropp, H [0000-0002-4258-3393], Lagergren, F [0000-0002-0061-733X], Lane, P [0000-0001-6121-8386], Lapenas, A [0000-0002-2135-3636], Lechuga, V [0000-0003-3745-587X], Lee,M [0000-0002-9601-3863], Leuschner, C [0000-0002-5689-7932], Limousin, JM [0000-0002-2734-2495], Linares, JC [0000-0001-8375-6353], Linderson, ML [0000-0001-6578-6671], Lindroth, A [0000-0002-7669-784X], Llorens, P [0000-0003-4591-5303], López-Bernal, A [0000-0002-1034-4718], Loranty, MM[0000-0001-8851-7386], Macinnis-Ng, C [0000-0003-3935-9814], Marechaux, I [0000-0002-5401-0197], Martin, TA [0000-0002-7872-4194], Matheny, A [0000-0002-9532-7131], McDowell, N [0000-0002-2178-2254], Meir, P [0000-0002-2362-0398], Mészáros, I [0000-0001-8841-730X], Migliavacca, M [0000-0003-3546-8407], Mölder, M [0000-0001-6767-3195], Montagnani, L [0000-0003-2957-9071], Moore, GW [0000-0001-5190-5983], Nakada, R [0000-0002-3704-1784], Niu, F [0000-0003-3445-4011], Nolan, R [0000-0001-9277-5142], Norby,R [0000-0002-0238-9828], Novick, K [0000-0002-8431-0879], Oberhuber, W [0000-0002-5197-7044], Obojes, N [0000-0002-6718-2756], Poyatos, R, Granda, V, Flo, V, Adams, MA, Adorján, B, Aguadé, D, Aidar, MPM, Allen, S, Alvarado-Barrientos, MS, Anderson-Teixeira, KJ, Aparecido, LM, Joly, CA, Kaplick, J, Kim, HS, Klemedtsson, L, Kropp, H, Lagergren, F, Lane, P, Lang, P, Lapenas, A, Lechuga, V, Migliavacca, M, Lee, M, Leuschner, C, Limousin, JM, Linares, JC, Linderson, ML, Lindroth, A, Llorens, P, López-Bernal, A, Loranty, MM, Lüttschwager, D, Mitchell, P, MacInnis-Ng, C, Maréchaux, I, Martin, TA, Matheny, A, McDowell, N, McMahon, S, Meir, P, Mészáros, I, Molder, M, Mölder, M, Montagnani, L, Moore, GW, Nakada, R, Niu, F, Nolan, R, Norby,R, Novick, K, Oberhuber, W, Obojes, N, Oishi, AC, Oliveira RS, Oren, R, Ourcival,JM, Paljakka, T, Perez-Priego, O, Peri, PL, Peters, RL, Pfautsch, S, Pockman, WT, Preisler, Y, Rascher, K, Robinson, G, Rocha, H, Rocheteau, A, Röll, A, Rosado, BHP, Rowland, L [, Rubtsov, A, Sabaté, S, Salmon, Y, Salomón, RL, Sánchez-Costa, E, Schäfer, K, Schuldt, B, Shashkin, A, Stahl, C, Stojanovic, M, Suárez, JC, Sun, G, Niu, FR, Szatniewska, J, Tatarinov, F, Tesar, M, Thomas, FM, Tor-ngern, P, Urban, J, Valladares, F, Van der Tol, C, Van Meerveld, Varlagin, A, Norby, R, Voigt, H, Warren, J, Werner, C, Werner, W, Wieser, G, Wingate, W, Wullschleger, S, Koong, Y, Zweifel, R, Arain, MA, Oliveira, RS, Ourcival, JM, Aranda, I, Roll, A, Asbjornsen, H, Baxter, R, Beamesderfer, E, Berry, ZC, Berveiller, D, Blakely, B, Boggs, J, Bohrer, G, Bolstad, PV, Bonal, D, Bracho, R, Brito, P, Brodeur, J, Casanoves, F, Chave, J, Chen, H, Cisneros, C, Clark, K, Cremonese, E, Dang, HZ, David, JS, David, TS, Delpierre, N, Desai, AR, Do, Frederic C., Dohnal, M, Domec, JC, Dzikiti, S, Edgar, C, Eichstaedt, R, El-Madany, TS, Elbers, J, Eller, CB, Euskirchen, ES, Ewers, B, Fonti, P, Forner, A, Forrester, DI, Freitas, HC, Galvagno, M, Garcia-Tejera, O, Ghimire, CP, Gimeno, TE, Grace, J, Granier, A, Griebel, A, Guangyu, Y, Gush, MB, Hanson, PJ, Hasselquist, NJ, Heinrich, I, Hernandez-Santana, V, Herrmann, V, Hölttä, T, Holwerda, F, Irvine, J, Ayutthaya, SIN, Jarvis, PG, Jochheim, H, Ministerio de Ciencia e Innovación (España), Agència de Gestió d'Ajuts Universitaris i de Recerca, Poyatos, R [0000-0003-0521-2523], Granda, V [0000-0002-0469-1991], Flo, V [0000-0003-1908-4577], Adams, MA [0000-0002-8154-0097], Adorjan, B [0000-0002-5482-2515], Aidar, MPM [0000-0001-5728-6749], Alvarado-Barrientos, MS [0000-0003-0098-0806], Anderson-Teixeira, KJ [0000-0001-7585-712X], Arain, MA [0000-0002-1433-5173], Aranda, I [0000-0001-9086-7940], Asbjornsen, H [000-0001-8126-3328], Oishi, AC [0000-0001-5064-4080], Oliveira RS [0000-0002-6392-2526], Oren, R [0000-0002-5654-1733], Ourcival,JM [0000-0002-3557-3496], Paljakka, T [0000-0002-3674-4904], Perez-Priego, O [0000-0002-3138-3177], Peri, PL [0000-0002-5398-4408], Peters, RL [0000-0002-7441-1297], Pfautsch, S [0000-0002-4390-4195], Pockman, WT [0000-0002-3286-0457], Baxter, R [0000-0002-7504-6797], Preisler, Y [0000-0001-5861-8362], Rocha, H [0000-0002-5981-4469], Röll, A [0000-0001-9457-4459], Rosado, BHP [0000-0002-8924-8672], Rowland, L [0000-0002-0774-3216], Rubtsov, A [0000-0002-9663-4344], Sabaté, S [0000-0003-1854-0761], Salmon, Y [0000-0003-4433-4021], Salomón, RL [0000-0003-2674-1731], Sánchez-Costa, E [0000-0001-6799-9611], Beamesderfer, E [0000-0002-7513-7349], Schäfer, K [0000-0001-9452-3619], Schuldt, B [0000-0003-4738-5289], Shashkin, A [0000-0001-9925-5019], Stahl, C [0000-0001-5411-1169], Stojanović, M [0000-0003-4918-8668], Sun, G [0000-0002-0159-1370], Szatniewska, J [0000-0003-3027-9965], Tatarinov, F [0000-0002-8338-6070], Tesar, M [0000-0002-5647-8498], Thomas, FM [0000-0001-6377-719X], Berveiller, D [0000-0001-7461-6420], Tor-ngern, P [0000-0001-7363-4926], Urban, J [0000-0003-1730-947X], Van der Tol, C [0000-0002-2484-8191], Van Meerveld [0000-0002-7547-3270], Varlagin, A [0000-0002-2549-5236], Werner, C [0000-0002-7676-9057], Wieser, G [0000-0002-7575-5657], Wingate, W [0000-0003-1921-1556], Wullschleger, S [0000-0002-9869-0446], Koong, Y [0000-0002-8630-3031], Blakely, B [0000-0001-9923-0794], Zweifel, R [0000-0001-9438-0582], Steppe, K [0000-0001-6252-0704], Mencuccini, M [0000-0003-0840-1477], Martínez-Vilalta, J [0000-0002-2332-7298], Boggs, J [0000-0003-4826-1843], Bohrer, G [0000-0002-9209-9540], Bolstad, P [0000-0002-1829-8859], Bonal, D [0000-0001-9602-8603], Bracho, R [0000-0002-8015-9796], Brodeur, J [0000-0001-7118-8360], Casanoves, F [0000-0001-8765-9382], Chave, J [0000-0002-7766-1347], Chen, H [0000-0001-7619-3425], Cisneros, C [0000-0001-9661-4581], Clark, K [0000-0003-0534-9677], Cremonese, E [0000-0002-6708-8532], Dang, H [0000-0003-4428-3834], David, J [0000-0001-6994-1085], David, T [0000-0003-1473-899X], Delpierre, D [0000-0003-0906-9402], Desai, AR [0000-0002-5226-6041], Do, FC [0000-0002-2852-627X], Dohnal, M [0000-0003-1769-4750], Domec, JC [0000-0003-0478-2559], Dzikiti, S [0000-0002-1892-4143], Edgar, C [0000-0002-7026-8358], Eichstaedt, R [0000-0002-4905-7994], El-Madany, T [0000-0002-0726-7141], Elbers, J [0000-0002-0631-3505], Eller, CB [0000-0002-7795-2574], Euskirchen, E [0000-0002-0848-4295], Ewers, B [0000-0001-6647-7475], Fonti, P [0000-0002-7070-3292], Forner, A [0000-0002-7123-6403], Forrester, D [0000-0003-2732-5692], Freitas, HC [0000-0002-4861-1164], Galvagno, M [0000-0002-0827-487X], Garcia-Tejera, O [0000-0001-7726-8118], Ghimire, CP [0000-0002-3715-6311], Gimeno, TE [0000-0002-1707-9291], Granier, A [0000-0002-4174-2487], Griebel, A [0000-0002-4476-8279], Guangyu, Y [0000-0003-3242-5348], Gush, MB [0000-0003-1328-9862], Hanson, PJ [0000-0001-7293-3561], Hasselquist, N [0000-0003-2777-0163], Heinrich, I [0000-0001-5800-6999], Hernandez-Santana, V [0000-0001-9018-8622], Herrmann, V [0000-0002-4519-481X], Hölttä, T [0000-0001-7677-7156], Holwerda, F [0000-0003-4125-1765], Ayutthaya, SIN [0000-0002-5354-1527], Jochheim,H [0000-0001-8047-4553], Joly, CA [0000-0002-7945-2805], Kim, HS [0000-0002-3440-6071], Klemedtsson, L [0000-0002-1122-0717], Kropp, H [0000-0002-4258-3393], Lagergren, F [0000-0002-0061-733X], Lane, P [0000-0001-6121-8386], Lapenas, A [0000-0002-2135-3636], Lechuga, V [0000-0003-3745-587X], Lee,M [0000-0002-9601-3863], Leuschner, C [0000-0002-5689-7932], Limousin, JM [0000-0002-2734-2495], Linares, JC [0000-0001-8375-6353], Linderson, ML [0000-0001-6578-6671], Lindroth, A [0000-0002-7669-784X], Llorens, P [0000-0003-4591-5303], López-Bernal, A [0000-0002-1034-4718], Loranty, MM[0000-0001-8851-7386], Macinnis-Ng, C [0000-0003-3935-9814], Marechaux, I [0000-0002-5401-0197], Martin, TA [0000-0002-7872-4194], Matheny, A [0000-0002-9532-7131], McDowell, N [0000-0002-2178-2254], Meir, P [0000-0002-2362-0398], Mészáros, I [0000-0001-8841-730X], Migliavacca, M [0000-0003-3546-8407], Mölder, M [0000-0001-6767-3195], Montagnani, L [0000-0003-2957-9071], Moore, GW [0000-0001-5190-5983], Nakada, R [0000-0002-3704-1784], Niu, F [0000-0003-3445-4011], Nolan, R [0000-0001-9277-5142], Norby,R [0000-0002-0238-9828], Novick, K [0000-0002-8431-0879], Oberhuber, W [0000-0002-5197-7044], Obojes, N [0000-0002-6718-2756], Poyatos, R, Granda, V, Flo, V, Adams, MA, Adorján, B, Aguadé, D, Aidar, MPM, Allen, S, Alvarado-Barrientos, MS, Anderson-Teixeira, KJ, Aparecido, LM, Joly, CA, Kaplick, J, Kim, HS, Klemedtsson, L, Kropp, H, Lagergren, F, Lane, P, Lang, P, Lapenas, A, Lechuga, V, Migliavacca, M, Lee, M, Leuschner, C, Limousin, JM, Linares, JC, Linderson, ML, Lindroth, A, Llorens, P, López-Bernal, A, Loranty, MM, Lüttschwager, D, Mitchell, P, MacInnis-Ng, C, Maréchaux, I, Martin, TA, Matheny, A, McDowell, N, McMahon, S, Meir, P, Mészáros, I, Molder, M, Mölder, M, Montagnani, L, Moore, GW, Nakada, R, Niu, F, Nolan, R, Norby,R, Novick, K, Oberhuber, W, Obojes, N, Oishi, AC, Oliveira RS, Oren, R, Ourcival,JM, Paljakka, T, Perez-Priego, O, Peri, PL, Peters, RL, Pfautsch, S, Pockman, WT, Preisler, Y, Rascher, K, Robinson, G, Rocha, H, Rocheteau, A, Röll, A, Rosado, BHP, Rowland, L [, Rubtsov, A, Sabaté, S, Salmon, Y, Salomón, RL, Sánchez-Costa, E, Schäfer, K, Schuldt, B, Shashkin, A, Stahl, C, Stojanovic, M, Suárez, JC, Sun, G, Niu, FR, Szatniewska, J, Tatarinov, F, Tesar, M, Thomas, FM, Tor-ngern, P, Urban, J, Valladares, F, Van der Tol, C, Van Meerveld, Varlagin, A, Norby, R, Voigt, H, Warren, J, Werner, C, Werner, W, Wieser, G, Wingate, W, Wullschleger, S, Koong, Y, Zweifel, R, Arain, MA, Oliveira, RS, Ourcival, JM, Aranda, I, Roll, A, Asbjornsen, H, Baxter, R, Beamesderfer, E, Berry, ZC, Berveiller, D, Blakely, B, Boggs, J, Bohrer, G, Bolstad, PV, Bonal, D, Bracho, R, Brito, P, Brodeur, J, Casanoves, F, Chave, J, Chen, H, Cisneros, C, Clark, K, Cremonese, E, Dang, HZ, David, JS, David, TS, Delpierre, N, Desai, AR, Do, Frederic C., Dohnal, M, Domec, JC, Dzikiti, S, Edgar, C, Eichstaedt, R, El-Madany, TS, Elbers, J, Eller, CB, Euskirchen, ES, Ewers, B, Fonti, P, Forner, A, Forrester, DI, Freitas, HC, Galvagno, M, Garcia-Tejera, O, Ghimire, CP, Gimeno, TE, Grace, J, Granier, A, Griebel, A, Guangyu, Y, Gush, MB, Hanson, PJ, Hasselquist, NJ, Heinrich, I, Hernandez-Santana, V, Herrmann, V, Hölttä, T, Holwerda, F, Irvine, J, Ayutthaya, SIN, Jarvis, PG, and Jochheim, H
- Abstract
Plant transpiration links physiological responses of vegetation to water supply and demand with hydrological, energy, and carbon budgets at the land-atmosphere interface. However, despite being the main land evaporative flux at the global scale, transpiration and its response to environmental drivers are currently not well constrained by observations. Here we introduce the first global compilation of whole-plant transpiration data from sap flow measurements (SAPFLUXNET, https://sapfluxnet.creaf.cat/, last access: 8 June 2021). We harmonized and quality-controlled individual datasets supplied by contributors worldwide in a semi-automatic data workflow implemented in the R programming language. Datasets include sub-daily time series of sap flow and hydrometeorological drivers for one or more growing seasons, as well as metadata on the stand characteristics, plant attributes, and technical details of the measurements. SAPFLUXNET contains 202 globally distributed datasets with sap flow time series for 2714 plants, mostly trees, of 174 species. SAPFLUXNET has a broad bioclimatic coverage, with woodland/shrubland and temperate forest biomes especially well represented (80% of the datasets). The measurements cover a wide variety of stand structural characteristics and plant sizes. The datasets encompass the period between 1995 and 2018, with 50% of the datasets being at least 3 years long. Accompanying radiation and vapour pressure deficit data are available for most of the datasets, while on-site soil water content is available for 56% of the datasets. Many datasets contain data for species that make up 90% or more of the total stand basal area, allowing the estimation of stand transpiration in diverse ecological settings. SAPFLUXNET adds to existing plant trait datasets, ecosystem flux networks, and remote sensing products to help increase our understanding of plant water use, plant responses to drought, and ecohydrological processes. SAPFLUXNET version 0.1.5 is freely a
- Published
- 2021
6. Global transpiration data from sap flow measurements: The SAPFLUXNET database
- Author
-
Poyatos, R, Granda, V, Flo, V, Adams, MA, Adorján, B, Aguadé, D, Aidar, MPM, Allen, S, Alvarado-Barrientos, MS, Anderson-Teixeira, KJ, Aparecido, LM, Joly, CA, Kaplick, J, Kim, HS, Klemedtsson, L, Kropp, H, Lagergren, F, Lane, P, Lang, P, Lapenas, A, Lechuga, V, Migliavacca, M, Lee, M, Leuschner, C, Limousin, JM, Linares, JC, Linderson, ML, Lindroth, A, Llorens, P, López-Bernal, A, Loranty, MM, Lüttschwager, D, Mitchell, P, MacInnis-Ng, C, Maréchaux, I, Martin, TA, Matheny, A, McDowell, N, McMahon, S, Meir, P, Mészáros, I, Molder, M, Mölder, M, Montagnani, L, Moore, GW, Nakada, R, Niu, F, Nolan, R, Norby,R, Novick, K, Oberhuber, W, Obojes, N, Oishi, AC, Oliveira RS, Oren, R, Ourcival,JM, Paljakka, T, Perez-Priego, O, Peri, PL, Peters, RL, Pfautsch, S, Pockman, WT, Preisler, Y, Rascher, K, Robinson, G, Rocha, H, Rocheteau, A, Röll, A, Rosado, BHP, Rowland, L [, Rubtsov, A, Sabaté, S, Salmon, Y, Salomón, RL, Sánchez-Costa, E, Schäfer, K, Schuldt, B, Shashkin, A, Stahl, C, Stojanovic, M, Suárez, JC, Sun, G, Niu, FR, Szatniewska, J, Tatarinov, F, Tesar, M, Thomas, FM, Tor-ngern, P, Urban, J, Valladares, F, Van der Tol, C, Van Meerveld, Varlagin, A, Norby, R, Voigt, H, Warren, J, Werner, C, Werner, W, Wieser, G, Wingate, W, Wullschleger, S, Koong, Y, Zweifel, R, Arain, MA, Oliveira, RS, Ourcival, JM, Aranda, I, Roll, A, Asbjornsen, H, Baxter, R, Beamesderfer, E, Berry, ZC, Berveiller, D, Blakely, B, Boggs, J, Bohrer, G, Bolstad, PV, Bonal, D, Bracho, R, Brito, P, Brodeur, J, Casanoves, F, Chave, J, Chen, H, Cisneros, C, Clark, K, Cremonese, E, Dang, HZ, David, JS, David, TS, Delpierre, N, Desai, AR, Do, Frederic C., Dohnal, M, Domec, JC, Dzikiti, S, Edgar, C, Eichstaedt, R, El-Madany, TS, Elbers, J, Eller, CB, Euskirchen, ES, Ewers, B, Fonti, P, Forner, A, Forrester, DI, Freitas, HC, Galvagno, M, Garcia-Tejera, O, Ghimire, CP, Gimeno, TE, Grace, J, Granier, A, Griebel, A, Guangyu, Y, Gush, MB, Hanson, PJ, Hasselquist, NJ, Heinrich, I, Hernandez-Santana, V, Herrmann, V, Hölttä, T, Holwerda, F, Irvine, J, Ayutthaya, SIN, Jarvis, PG, Jochheim, H, Ministerio de Ciencia e Innovación (España), Agència de Gestió d'Ajuts Universitaris i de Recerca, Poyatos, R [0000-0003-0521-2523], Granda, V [0000-0002-0469-1991], Flo, V [0000-0003-1908-4577], Adams, MA [0000-0002-8154-0097], Adorjan, B [0000-0002-5482-2515], Aidar, MPM [0000-0001-5728-6749], Alvarado-Barrientos, MS [0000-0003-0098-0806], Anderson-Teixeira, KJ [0000-0001-7585-712X], Arain, MA [0000-0002-1433-5173], Aranda, I [0000-0001-9086-7940], Asbjornsen, H [000-0001-8126-3328], Oishi, AC [0000-0001-5064-4080], Oliveira RS [0000-0002-6392-2526], Oren, R [0000-0002-5654-1733], Ourcival,JM [0000-0002-3557-3496], Paljakka, T [0000-0002-3674-4904], Perez-Priego, O [0000-0002-3138-3177], Peri, PL [0000-0002-5398-4408], Peters, RL [0000-0002-7441-1297], Pfautsch, S [0000-0002-4390-4195], Pockman, WT [0000-0002-3286-0457], Baxter, R [0000-0002-7504-6797], Preisler, Y [0000-0001-5861-8362], Rocha, H [0000-0002-5981-4469], Röll, A [0000-0001-9457-4459], Rosado, BHP [0000-0002-8924-8672], Rowland, L [0000-0002-0774-3216], Rubtsov, A [0000-0002-9663-4344], Sabaté, S [0000-0003-1854-0761], Salmon, Y [0000-0003-4433-4021], Salomón, RL [0000-0003-2674-1731], Sánchez-Costa, E [0000-0001-6799-9611], Beamesderfer, E [0000-0002-7513-7349], Schäfer, K [0000-0001-9452-3619], Schuldt, B [0000-0003-4738-5289], Shashkin, A [0000-0001-9925-5019], Stahl, C [0000-0001-5411-1169], Stojanović, M [0000-0003-4918-8668], Sun, G [0000-0002-0159-1370], Szatniewska, J [0000-0003-3027-9965], Tatarinov, F [0000-0002-8338-6070], Tesar, M [0000-0002-5647-8498], Thomas, FM [0000-0001-6377-719X], Berveiller, D [0000-0001-7461-6420], Tor-ngern, P [0000-0001-7363-4926], Urban, J [0000-0003-1730-947X], Van der Tol, C [0000-0002-2484-8191], Van Meerveld [0000-0002-7547-3270], Varlagin, A [0000-0002-2549-5236], Werner, C [0000-0002-7676-9057], Wieser, G [0000-0002-7575-5657], Wingate, W [0000-0003-1921-1556], Wullschleger, S [0000-0002-9869-0446], Koong, Y [0000-0002-8630-3031], Blakely, B [0000-0001-9923-0794], Zweifel, R [0000-0001-9438-0582], Steppe, K [0000-0001-6252-0704], Mencuccini, M [0000-0003-0840-1477], Martínez-Vilalta, J [0000-0002-2332-7298], Boggs, J [0000-0003-4826-1843], Bohrer, G [0000-0002-9209-9540], Bolstad, P [0000-0002-1829-8859], Bonal, D [0000-0001-9602-8603], Bracho, R [0000-0002-8015-9796], Brodeur, J [0000-0001-7118-8360], Casanoves, F [0000-0001-8765-9382], Chave, J [0000-0002-7766-1347], Chen, H [0000-0001-7619-3425], Cisneros, C [0000-0001-9661-4581], Clark, K [0000-0003-0534-9677], Cremonese, E [0000-0002-6708-8532], Dang, H [0000-0003-4428-3834], David, J [0000-0001-6994-1085], David, T [0000-0003-1473-899X], Delpierre, D [0000-0003-0906-9402], Desai, AR [0000-0002-5226-6041], Do, FC [0000-0002-2852-627X], Dohnal, M [0000-0003-1769-4750], Domec, JC [0000-0003-0478-2559], Dzikiti, S [0000-0002-1892-4143], Edgar, C [0000-0002-7026-8358], Eichstaedt, R [0000-0002-4905-7994], El-Madany, T [0000-0002-0726-7141], Elbers, J [0000-0002-0631-3505], Eller, CB [0000-0002-7795-2574], Euskirchen, E [0000-0002-0848-4295], Ewers, B [0000-0001-6647-7475], Fonti, P [0000-0002-7070-3292], Forner, A [0000-0002-7123-6403], Forrester, D [0000-0003-2732-5692], Freitas, HC [0000-0002-4861-1164], Galvagno, M [0000-0002-0827-487X], Garcia-Tejera, O [0000-0001-7726-8118], Ghimire, CP [0000-0002-3715-6311], Gimeno, TE [0000-0002-1707-9291], Granier, A [0000-0002-4174-2487], Griebel, A [0000-0002-4476-8279], Guangyu, Y [0000-0003-3242-5348], Gush, MB [0000-0003-1328-9862], Hanson, PJ [0000-0001-7293-3561], Hasselquist, N [0000-0003-2777-0163], Heinrich, I [0000-0001-5800-6999], Hernandez-Santana, V [0000-0001-9018-8622], Herrmann, V [0000-0002-4519-481X], Hölttä, T [0000-0001-7677-7156], Holwerda, F [0000-0003-4125-1765], Ayutthaya, SIN [0000-0002-5354-1527], Jochheim,H [0000-0001-8047-4553], Joly, CA [0000-0002-7945-2805], Kim, HS [0000-0002-3440-6071], Klemedtsson, L [0000-0002-1122-0717], Kropp, H [0000-0002-4258-3393], Lagergren, F [0000-0002-0061-733X], Lane, P [0000-0001-6121-8386], Lapenas, A [0000-0002-2135-3636], Lechuga, V [0000-0003-3745-587X], Lee,M [0000-0002-9601-3863], Leuschner, C [0000-0002-5689-7932], Limousin, JM [0000-0002-2734-2495], Linares, JC [0000-0001-8375-6353], Linderson, ML [0000-0001-6578-6671], Lindroth, A [0000-0002-7669-784X], Llorens, P [0000-0003-4591-5303], López-Bernal, A [0000-0002-1034-4718], Loranty, MM[0000-0001-8851-7386], Macinnis-Ng, C [0000-0003-3935-9814], Marechaux, I [0000-0002-5401-0197], Martin, TA [0000-0002-7872-4194], Matheny, A [0000-0002-9532-7131], McDowell, N [0000-0002-2178-2254], Meir, P [0000-0002-2362-0398], Mészáros, I [0000-0001-8841-730X], Migliavacca, M [0000-0003-3546-8407], Mölder, M [0000-0001-6767-3195], Montagnani, L [0000-0003-2957-9071], Moore, GW [0000-0001-5190-5983], Nakada, R [0000-0002-3704-1784], Niu, F [0000-0003-3445-4011], Nolan, R [0000-0001-9277-5142], Norby,R [0000-0002-0238-9828], Novick, K [0000-0002-8431-0879], Oberhuber, W [0000-0002-5197-7044], and Obojes, N [0000-0002-6718-2756]
- Subjects
Stomatal condua ,Sapflow measurements ,Heat-pulse method ,Vapor- pressure deficit ,Radial patterns ,Water use strategies ,Eddy covariance ,Fluw density ,Thermal dissipation - Abstract
Plant transpiration links physiological responses of vegetation to water supply and demand with hydrological, energy, and carbon budgets at the land-atmosphere interface. However, despite being the main land evaporative flux at the global scale, transpiration and its response to environmental drivers are currently not well constrained by observations. Here we introduce the first global compilation of whole-plant transpiration data from sap flow measurements (SAPFLUXNET, https://sapfluxnet.creaf.cat/, last access: 8 June 2021). We harmonized and quality-controlled individual datasets supplied by contributors worldwide in a semi-automatic data workflow implemented in the R programming language. Datasets include sub-daily time series of sap flow and hydrometeorological drivers for one or more growing seasons, as well as metadata on the stand characteristics, plant attributes, and technical details of the measurements. SAPFLUXNET contains 202 globally distributed datasets with sap flow time series for 2714 plants, mostly trees, of 174 species. SAPFLUXNET has a broad bioclimatic coverage, with woodland/shrubland and temperate forest biomes especially well represented (80% of the datasets). The measurements cover a wide variety of stand structural characteristics and plant sizes. The datasets encompass the period between 1995 and 2018, with 50% of the datasets being at least 3 years long. Accompanying radiation and vapour pressure deficit data are available for most of the datasets, while on-site soil water content is available for 56% of the datasets. Many datasets contain data for species that make up 90% or more of the total stand basal area, allowing the estimation of stand transpiration in diverse ecological settings. SAPFLUXNET adds to existing plant trait datasets, ecosystem flux networks, and remote sensing products to help increase our understanding of plant water use, plant responses to drought, and ecohydrological processes. SAPFLUXNET version 0.1.5 is freely available from the Zenodo repository (10.5281/zenodo.3971689; Poyatos et al., 2020a). The "sapfluxnetr"R package-designed to access, visualize, and process SAPFLUXNET data-is available from CRAN. This research was supported by the Ministerio de Economía y Competitividad (grant no. CGL2014-55883-JIN), the Ministerio de Ciencia e Innovación (grant no. RTI2018-095297-J-I00), the Ministerio de Ciencia e Innovación (grant no. CAS16/00207), the Agència de Gestió d'Ajuts Universitaris i de Recerca (grant no. SGR1001), the Alexander von Humboldt-Stiftung (Humboldt Research Fellowship for Experienced Researchers (RP)), and the Institució Catalana de Recerca i Estudis Avançats (Academia Award (JMV)). Víctor Flo was supported by the doctoral fellowship FPU15/03939 (MECD, Spain).
- Published
- 2021
7. Global transpiration data from sap flow measurements: The SAPFLUXNET database
- Author
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Poyatos, R., Granda, V, Flo, V., Adorján, B., Adams, M. A., Aguadé, D., Aidar, M. P. M., Allen, S., Alvarado-Barrientos, M. S., Anderson-Teixeira, K. J., Aparecido, L. M., Altaf Arain, M., Aranda, I., Asbjornsen, H., Baxter, R., Beamesderfer, E., Berry, Z. C., Berveiller, D., Blakely, B., Boggs, J., Bohrer, G., Bolstad, P. V., Bonal, D., Bracho, R., Brito, P., Brodeur, J., Casanoves, F., Chave, J., Chen, H., Cisneros, C., Clark, K., Cremonese, E., Dang, H., David, J. S., David, T. S., Delpierre, N., Desai, A. R., Do, F. C., Dohnal, N., Domec, J. C., Dzikiti, S., Edgar, C., Eichstaedt, R., El-Madany, T. S., Elbers, J., Eller, C. B., Euskirchen, E. S., Ewers, B., Fonti, P., Forner, A., Forrester, D. I., Freitas, H. C., Galvagno, M., Garcia-Tejera, O., Ghimire, C. P., Gimeno, T. E., Grace, J., Granier, A., Griebel, A., Guangyu, Y., Gush, M. B., Hanson, P. J., Hasselquist, N. J., Heinrich, I., Hernandez-Santana, V., Herrmann, V, Hölttä, T., Holwerda, F., Irvine, J., Na Ayutthaya, S. Y., Jarvis, P. J., Jochheim, H., Joly, C. A., Kaplick, J., Kim, H. S., Klemedtsson, L., Kropp, H., Lagergren, F., Lane, P., Lang, P., Lapenas, A., Lechuga, V., Lee, M., Leuschner, C., Limousin, J. M., Linares, J. C., Linderson, M. L., Lindroth, A., Llorens, P., López-Bernal, A., Loranty, M. M., Lüttschwager, D., MacInnis-Ng, C., Maréchaux, I., Martin, T. A., Matheny, A., McDowell, N., McMahon, S., Meir, P., Mészáros, I., Migliavacca, M., Mitchell, P., Mölder, M., Montagnani, L., Moore, G. W., Nakada, R., Niu, F., Nolan, R.H., Norby, R., Novick, K., Oberhuber, W., Obojes, N., Oishi, A. C., Oliveira, R. S., Olen, R., Ourcival, J. M., Paljakka, T., Perez Priego, O., Peri, P. L., Peters, R. L., Pfautsch, S., Pockman, W. T., Preysler, I., Rascher, K., Robinson, G., Rocheteau, A., Rocha, H., Röll, A., Rosado, B. H. P., Rowland, L., Rubtsov, A. V., Sabaté, S., Salmón, Y., Salomon, R. L., Schäfer, K. V. R., Sánchez-Costa, E., Schuld, B., Shashkin, A., Stahl, C., Stojanovic, M., Suárez, J. C., Szatniewska, J, Sun, G., Tatarinov, F., TesaÅ, M, Thomas, F. M., Tor-Ngern, P., Urban, J., Valladares, F., Van Der Tol, C., Van Meerveld, I., Varlagin, A., Voigt, H., Warren, J., Werner, C., Poyatos, R., Granda, V, Flo, V., Adorján, B., Adams, M. A., Aguadé, D., Aidar, M. P. M., Allen, S., Alvarado-Barrientos, M. S., Anderson-Teixeira, K. J., Aparecido, L. M., Altaf Arain, M., Aranda, I., Asbjornsen, H., Baxter, R., Beamesderfer, E., Berry, Z. C., Berveiller, D., Blakely, B., Boggs, J., Bohrer, G., Bolstad, P. V., Bonal, D., Bracho, R., Brito, P., Brodeur, J., Casanoves, F., Chave, J., Chen, H., Cisneros, C., Clark, K., Cremonese, E., Dang, H., David, J. S., David, T. S., Delpierre, N., Desai, A. R., Do, F. C., Dohnal, N., Domec, J. C., Dzikiti, S., Edgar, C., Eichstaedt, R., El-Madany, T. S., Elbers, J., Eller, C. B., Euskirchen, E. S., Ewers, B., Fonti, P., Forner, A., Forrester, D. I., Freitas, H. C., Galvagno, M., Garcia-Tejera, O., Ghimire, C. P., Gimeno, T. E., Grace, J., Granier, A., Griebel, A., Guangyu, Y., Gush, M. B., Hanson, P. J., Hasselquist, N. J., Heinrich, I., Hernandez-Santana, V., Herrmann, V, Hölttä, T., Holwerda, F., Irvine, J., Na Ayutthaya, S. Y., Jarvis, P. J., Jochheim, H., Joly, C. A., Kaplick, J., Kim, H. S., Klemedtsson, L., Kropp, H., Lagergren, F., Lane, P., Lang, P., Lapenas, A., Lechuga, V., Lee, M., Leuschner, C., Limousin, J. M., Linares, J. C., Linderson, M. L., Lindroth, A., Llorens, P., López-Bernal, A., Loranty, M. M., Lüttschwager, D., MacInnis-Ng, C., Maréchaux, I., Martin, T. A., Matheny, A., McDowell, N., McMahon, S., Meir, P., Mészáros, I., Migliavacca, M., Mitchell, P., Mölder, M., Montagnani, L., Moore, G. W., Nakada, R., Niu, F., Nolan, R.H., Norby, R., Novick, K., Oberhuber, W., Obojes, N., Oishi, A. C., Oliveira, R. S., Olen, R., Ourcival, J. M., Paljakka, T., Perez Priego, O., Peri, P. L., Peters, R. L., Pfautsch, S., Pockman, W. T., Preysler, I., Rascher, K., Robinson, G., Rocheteau, A., Rocha, H., Röll, A., Rosado, B. H. P., Rowland, L., Rubtsov, A. V., Sabaté, S., Salmón, Y., Salomon, R. L., Schäfer, K. V. R., Sánchez-Costa, E., Schuld, B., Shashkin, A., Stahl, C., Stojanovic, M., Suárez, J. C., Szatniewska, J, Sun, G., Tatarinov, F., TesaÅ, M, Thomas, F. M., Tor-Ngern, P., Urban, J., Valladares, F., Van Der Tol, C., Van Meerveld, I., Varlagin, A., Voigt, H., Warren, J., and Werner, C.
- Abstract
Plant transpiration links physiological responses of vegetation to water supply and demand with hydrological, energy, and carbon budgets at the land-atmosphere interface. However, despite being the main land evaporative flux at the global scale, transpiration and its response to environmental drivers are currently not well constrained by observations. Here we introduce the first global compilation of whole-plant transpiration data from sap flow measurements (SAPFLUXNET, https://sapfluxnet.creaf.cat/, last access: 8 June 2021). We harmonized and quality-controlled individual datasets supplied by contributors worldwide in a semi-automatic data workflow implemented in the R programming language. Datasets include sub-daily time series of sap flow and hydrometeorological drivers for one or more growing seasons, as well as metadata on the stand characteristics, plant attributes, and technical details of the measurements. SAPFLUXNET contains 202 globally distributed datasets with sap flow time series for 2714 plants, mostly trees, of 174 species. SAPFLUXNET has a broad bioclimatic coverage, with woodland/shrubland and temperate forest biomes especially well represented (80% of the datasets). The measurements cover a wide variety of stand structural characteristics and plant sizes. The datasets encompass the period between 1995 and 2018, with 50% of the datasets being at least 3 years long. Accompanying radiation and vapour pressure deficit data are available for most of the datasets, while on-site soil water content is available for 56% of the datasets. Many datasets contain data for species that make up 90% or more of the total stand basal area, allowing the estimation of stand transpiration in diverse ecological settings. SAPFLUXNET adds to existing plant trait datasets, ecosystem flux networks, and remote sensing products to help increase our understanding of plant water use, plant responses to drought, and ecohydrological processes. SAPFLUXNET version 0.1.5 is freely a
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- 2021
8. Drought effects on carbon allocation to resin defences and on resin dynamics in old-grown Scots pine
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Rissanen, K., primary, Hölttä, T., additional, Bäck, J., additional, Rigling, A., additional, Wermelinger, B., additional, and Gessler, A., additional
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- 2021
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9. Modeling xylem and phloem water flows in trees according to cohesion theory and Münch hypothesis
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Hölttä, T., Vesala, T., Sevanto, S., Perämäki, M., and Nikinmaa, E.
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- 2006
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10. Is decreased xylem sap surface tension associated with embolism and loss of xylem hydraulic conductivity in pathogen-infected Norway spruce saplings?
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Paljakka, T. (Teemu), Rissanen, K. (Kaisa), Vanhatalo, A. (Anni), Salmon, Y. (Yann), Jyske, T. (Tuula), Prisle, N. L. (Nønne L.), Linnakoski, R. (Riikka), Lin, J. J. (Jack J.), Laakso, T. (Tapio), Kasanen, R. (Risto), Bäck, J. (Jaana), Hölttä, T. (Teemu), Paljakka, T. (Teemu), Rissanen, K. (Kaisa), Vanhatalo, A. (Anni), Salmon, Y. (Yann), Jyske, T. (Tuula), Prisle, N. L. (Nønne L.), Linnakoski, R. (Riikka), Lin, J. J. (Jack J.), Laakso, T. (Tapio), Kasanen, R. (Risto), Bäck, J. (Jaana), and Hölttä, T. (Teemu)
- Abstract
Increased abiotic stress along with increasing temperatures, dry periods and forest disturbances may favor biotic stressors such as simultaneous invasion of bark beetle and ophiostomatoid fungi. It is not fully understood how tree desiccation is associated with colonization of sapwood by fungi. A decrease in xylem sap surface tension (σxylem) as a result of infection has been hypothesized to cause xylem embolism by lowering the threshold for air-seeding at the pits between conduits and disruptions in tree water transport. However, this hypothesis has not yet been tested. We investigated tree water relations by measuring the stem xylem hydraulic conductivity (Kstem), σxylem, stem relative water content (RWCstem), and water potential (Ψstem), and canopy conductance (gcanopy), as well as the compound composition in xylem sap in Norway spruce (Picea abies) saplings. We conducted our measurements at the later stage of Endoconidiophora polonica infection when visible symptoms had occurred in xylem. Saplings of two clones (44 trees altogether) were allocated to treatments of inoculated, wounded control and intact control trees in a greenhouse. The saplings were destructively sampled every second week during summer 2016. σxylem, Kstem and RWCstem decreased following the inoculation, which may indicate that decreased σxylem resulted in increased embolism. gcanopy did not differ between treatments indicating that stomata responded to Ψstem rather than to embolism formation. Concentrations of quinic acid, myo-inositol, sucrose and alkylphenol increased in the xylem sap of inoculated trees. Myo-inositol concentrations also correlated negatively with σxylem and Kstem. Our study is a preliminary investigation of the role of σxylem in E. polonica infected trees based on previous hypotheses. The results suggest that E. polonica infection can lead to a simultaneous decrease in xylem sap surface tension and a decline in tree hydraulic conductivity, thus hampering tree water
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- 2020
11. Transport in xylem sap affects the emissions of acetaldehyde from Scots pine stem
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Rissanen, K., primary, Aalto, J., additional, Bäck, J., additional, and Hölttä, T., additional
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- 2020
- Full Text
- View/download PDF
12. Hypertension, cardiac state, and the role of volume overload during peritoneal dialysis
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Hölttä, T., Happonen, Juha-Matti, Rönnholm, K., Fyhrquist, Frej, and Holmberg, Christer
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- 2001
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13. Quantifying in situ phenotypic variability in the hydraulic properties of four tree species across their distribution range in Europe
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González-Muñoz, N., Sterck, F., Torres-Ruiz, J.M., Petit, G., Cochard, H., von Arx, G., Lintunen, A., Caldeira, M.C., Capdeville, G., Copini, P., Gebauer, R., Grönlund, L., Hölttä, T., Lobo-do-Vale, R., Peltoniemi, M., Stritih, A., Urban, J., Delzon, S., González-Muñoz, N., Sterck, F., Torres-Ruiz, J.M., Petit, G., Cochard, H., von Arx, G., Lintunen, A., Caldeira, M.C., Capdeville, G., Copini, P., Gebauer, R., Grönlund, L., Hölttä, T., Lobo-do-Vale, R., Peltoniemi, M., Stritih, A., Urban, J., and Delzon, S.
- Abstract
Many studies have reported that hydraulic properties vary considerably between tree species, but little is known about their intraspecific variation and, therefore, their capacity to adapt to a warmer and drier climate. Here, we quantify phenotypic divergence and clinal variation for embolism resistance, hydraulic conductivity and branch growth, in four tree species, two angiosperms (Betula pendula, Populus tremula) and two conifers (Picea abies, Pinus sylvestris), across their latitudinal distribution in Europe. Growth and hydraulic efficiency varied widely within species and between populations. The variability of embolism resistance was in general weaker than that of growth and hydraulic efficiency, and very low for all species but Populus tremula. In addition, no and weak support for a safety vs. efficiency trade-off was observed for the angiosperm and conifer species, respectively. The limited variability of embolism resistance observed here for all species except Populus tremula, suggests that forest populations will unlikely be able to adapt hydraulically to drier conditions through the evolution of embolism resistance.
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- 2018
14. Belowground hydraulic conductance in a mature boreal Scots pine tree
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Lintunen, A., primary, Paljakka, T., additional, Salmon, Y., additional, and Hölttä, T., additional
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- 2018
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15. Silver birch ability to refill fully embolised xylem conduits under tension
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Salmon, Y., primary, Lintunen, A., additional, Lindfors, L., additional, Suhonen, H., additional, Sevanto, S., additional, Vesala, T., additional, and Hölttä, T., additional
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- 2018
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16. Transpiration directly regulates the emissions of water-soluble short-chained OVOCs
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Rissanen, K., primary, Hölttä, T., additional, and Bäck, J., additional
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- 2018
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17. Water relations in silver birch during springtime: How is sap pressurised?
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Hölttä, T., primary, Dominguez Carrasco, M. D. R., additional, Salmon, Y., additional, Aalto, J., additional, Vanhatalo, A., additional, Bäck, J., additional, and Lintunen, A., additional
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- 2018
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18. Quantifying in situ phenotypic variability in the hydraulic properties of four tree species across their distribution range in Europe
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González-Muñoz, N., primary, Sterck, F., additional, Torres-Ruiz, J. M., additional, Petit, G., additional, Cochard, H., additional, von Arx, G., additional, Lintunen, A., additional, Caldeira, M. C., additional, Capdeville, G., additional, Copini, P., additional, Gebauer, R., additional, Grönlund, L., additional, Hölttä, T., additional, Lobo-do-Vale, R., additional, Peltoniemi, M., additional, Stritih, A., additional, Urban, J., additional, and Delzon, S., additional
- Published
- 2018
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19. Effects of competition, drought stress and photosynthetic productivity on the radial growth of white spruce in western Canada
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Alam, S. A., Huang, J. G., Stadt, K. J., Comeau, P. G., Dawson, A., Gea Izquierdo, Guillermo, Aakala, T., Hölttä, T., Vesala, T., Mäkelä, A., Berninger, F., Alam, S. A., Huang, J. G., Stadt, K. J., Comeau, P. G., Dawson, A., Gea Izquierdo, Guillermo, Aakala, T., Hölttä, T., Vesala, T., Mäkelä, A., and Berninger, F.
- Abstract
Understanding the complex interactions of competition, climate warming-induced drought stress, and photosynthetic productivity on the radial growth of trees is central to linking climate change impacts on tree growth, stand structure and in general, forest productivity. Using a mixed modeling approach, a stand-level photosynthetic production model, climate, stand competition and tree-ring data from mixedwood stands in western Canada, we investigated the radial growth response of white spruce [Picea glauca (Moench.) Voss] to simulated annual photosynthetic production, simulated drought stress, and tree and stand level competition. The long-term (~80-year) radial growth of white spruce was constrained mostly by competition, as measured by total basal area, with minor effects from drought. There was no relation of competition and drought on tree growth but dominant trees increased their growth more strongly to increases in modeled photosynthetic productivity, indicating asymmetric competition. Our results indicate a co-limitation of drought and climatic factors inhibiting photosynthetic productivity for radial growth of white spruce in western Canada. These results illustrate how a modeling approach can separate the complex factors regulating both multi-decadal average radial growth and interannual radial growth variations of white spruce, and contribute to advance our understanding on sustainable management of mixedwood boreal forests in western Canada. © 2017 Alam, Huang, Stadt, Comeau, Dawson, Gea-Izquierdo, Aakala, Hölttä, Vesala, Mäkelä and Berninger.
- Published
- 2017
20. Diurnal patterns in Scots pine stem oleoresin pressure in a boreal forest
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Rissanen, K., primary, Hölttä, T., additional, Vanhatalo, A., additional, Aalto, J., additional, Nikinmaa, E., additional, Rita, H., additional, and Bäck, J., additional
- Published
- 2015
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21. Tree water relations can trigger monoterpene emissions from Scots pine stems during spring recovery
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Vanhatalo, A., primary, Chan, T., additional, Aalto, J., additional, Korhonen, J. F., additional, Kolari, P., additional, Hölttä, T., additional, Nikinmaa, E., additional, and Bäck, J., additional
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- 2015
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22. Tree water relations trigger monoterpene emissions from Scots pine stem during spring recovery
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Vanhatalo, A., primary, Chan, T., additional, Aalto, J., additional, Korhonen, J. F., additional, Kolari, P., additional, Hölttä, T., additional, Nikinmaa, E., additional, and Bäck, J., additional
- Published
- 2015
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23. Anatomical regulation of ice nucleation and cavitation helps trees to survive freezing and drought stress
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Lintunen, A., primary, Hölttä, T., additional, and Kulmala, M., additional
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- 2013
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24. MODELLING THE EFFECT OF XYLEM AND PHLOEM TRANSPORT ON LEAF GAS EXCHANGE
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Hölttä, T., primary and Nikinmaa, E., additional
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- 2013
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25. Diurnal patterns in Scots pine stem oleoresin pressure in a boreal forest.
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Rissanen, K., Hölttä, T., Vanhatalo, A., Aalto, J., Nikinmaa, E., Rita, H., and Bäck, J.
- Subjects
- *
SCOTS pine , *OLEORESINS , *PLANT stems , *TAIGA ecology , *PLANT transpiration , *XYLEM , *SOIL moisture - Abstract
Coniferous tree stems contain large amounts of oleoresin under positive pressure in the resin ducts. Studies in North-American pines indicated that the stem oleoresin exudation pressure (OEP) correlates negatively with transpiration rate and soil water content. However, it is not known how the OEP changes affect the emissions of volatile vapours from the trees. We measured the OEP, xylem diameter changes indicating changes in xylem water potential and monoterpene emissions under field conditions in mature Scots pine ( Pinus sylvestris L.) trees in southern Finland. Contrary to earlier reports, the diurnal OEP changes were positively correlated with temperature and transpiration rate. OEP was lowest at the top part of the stem, where water potentials were also more negative, and often closely linked to ambient temperature and stem monoterpene emissions. However, occasionally OEP was affected by sudden changes in vapour pressure deficit (VPD), indicating the importance of xylem water potential on OEP as well. We conclude that the oleoresin storage pools in tree stems are in a dynamic relationship with ambient temperature and xylem water potential, and that the canopy monoterpene emission rates may therefore be also regulated by whole tree processes and not only by the conditions prevailing in the upper canopy. [ABSTRACT FROM AUTHOR]
- Published
- 2016
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26. THE EFFECTS OF HEAT STORAGE DURING LOW FLOW RATES ON THE OUTPUT OF GRANIER-TYPE SAP-FLOW SENSORS
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Sevanto, S., primary, Hölttä, T., additional, and Nikinmaa, E., additional
- Published
- 2009
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27. Linking phloem function to structure: Analysis with a coupled xylem–phloem transport model
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Hölttä, T., primary, Mencuccini, M., additional, and Nikinmaa, E., additional
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- 2009
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28. A model of bubble growth leading to xylem conduit embolism
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Hölttä, T., primary, Vesala, T., additional, and Nikinmaa, E., additional
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- 2007
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29. Tree water relations trigger monoterpene emissions from Scots pine stem during spring recovery.
- Author
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Vanhatalo, A., Chan, T., Aalto, J., Korhonen, J. F., Kolari, P., Hölttä, T., Nikinmaa, E., and Bäck, J.
- Subjects
MONOTERPENES ,WATER requirements for trees ,EMISSIONS (Air pollution) ,SCOTS pine ,SPRING ,VOLATILE organic compounds - Abstract
Tree canopies are known to emit large amounts of VOCs (volatile organic compounds) such as monoterpenes to the surrounding air. The main source for these is considered to be the green biomass, i.e. foliage, but emissions from the woody compartments have not been quantified. A VOC emission anomaly has been observed during transition from winter to summer activity. We analyzed if non-foliar components could partially explain the anomaly. We measured the VOC emissions from Scots pine (Pinus sylvestris L.) stems and shoots during the dehardening phase of trees in field conditions in two consecutive springs. We observed a large, transient monoterpene burst from stems, while the shoot monoterpene emissions and transpiration remained low. The burst lasted about 12 h. Simultaneously, an unusual night-time sap flow and an anomalous diurnal pattern of tree diameter were detected. Hence, we suggest that the monoterpene burst was a consequence of the recovery of the stem from winter-time. This indicates that the dominant processes and environmental drivers triggering the monoterpene emissions are different between stems and foliage. [ABSTRACT FROM AUTHOR]
- Published
- 2015
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- View/download PDF
30. Modeling xylem and phloem water flows in trees according to cohesion theory and Münch hypothesis
- Author
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Hölttä, T., primary, Vesala, T., additional, Sevanto, S., additional, Perämäki, M., additional, and Nikinmaa, E., additional
- Published
- 2005
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31. Relationships between Embolism, Stem Water Tension, and Diameter Changes
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HÖLTTÄ, T., primary, VESALA, T., additional, PERÄMÄKI, M., additional, and NIKINMAA, E., additional
- Published
- 2002
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32. Renal manifestations of Henoch-Schonlein purpura in a 6-month prospective study of 223 children.
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Jauhola O, Ronkainen J, Koskimies O, Ala-Houhala M, Arikoski P, Hölttä T, Jahnukainen T, Rajantie J, Ormälä T, Turtinen J, and Nuutinen M
- Abstract
Objective To assess the risk factors for developing Henoch-Schönlein purpura nephritis (HSN) and to determine the time period when renal involvement is unlikely after the initial disease onset. Design A prospective study of 223 paediatric patients to examine renal manifestations of Henoch-Schönlein purpura (HSP). The patient's condition was monitored with five outpatient visits to the research centre and urine dipstick testing at home. Results HSN occurred in 102/223 (46%) patients, consisting of isolated haematuria in 14%, isolated proteinuria in 9%, both haematuria and proteinuria in 56%, nephrotic-range proteinuria in 20% and nephrotic-nephritic syndrome in 1%. The patients who developed HSN were significantly older than those who did not (8.2±3.8 vs 6.2±3.0 years, p<0.001, CI for the difference 1.1 to 2.9). Nephritis occurred a mean of 14 days after HSP diagnosis, and within 1 month in the majority of cases. The risk of developing HSN after 2 months was 2%. Prednisone prophylaxis did not affect the timing of the appearance of nephritis. The risk factors for developing nephritis were age over 8 years at onset (OR 2.7, p=0.002, CI 1.4 to 5.1), abdominal pain (OR 2.1, p=0.017, CI 1.1 to 3.7) and recurrence of HSP disease (OR 3.1, p=0.002, CI 1.5 to 6.3). Patients with two or three risk factors developed nephritis in 63% and 87% of cases, respectively. Laboratory tests or blood pressure measurement at onset did not predict the occurrence of nephritis. Conclusion The authors recommend weekly home urine dipstick analyses for the first 2 months for patients with HSP. Patients with nephritis should be followed up for more than 6 months as well as the patients with HSP recurrence. [ABSTRACT FROM AUTHOR]
- Published
- 2010
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33. Clinical course of extrarenal symptoms in Henoch-Schonlein purpura: a 6-month prospective study.
- Author
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Jauhola O, Ronkainen J, Koskimies O, Ala-Houhala M, Arikoski P, Hölttä T, Jahnukainen T, Rajantie J, Ormälä T, and Nuutinen M
- Abstract
Objective To describe the extrarenal symptoms and clinical course of Henoch-Schönlein purpura (HSP). Design A prospective national multicentre trial with 6-month follow-up. Patients A total of 223 newly diagnosed paediatric HSP patients. Results Purpura was the initial symptom in 73% of the patients and was preceded by joint or gastrointestinal manifestations in the rest by a mean of 4 days. Joint symptoms, abdominal pain, melena, nephritis and recurrences occurred in 90%, 57%, 8%, 46% and 25% of the patients, respectively. Orchitis affected 17/122 (14%) of the boys. Seven patients developed protein-losing enteropathy characterised by abdominal pain, oedema and serum albumin under 30 g/l, and an additional 49 patients had subnormal albumin levels without any proteinuria. Positive fecal occult blood (26/117, 22%) and [alpha]1-antitrypsin (7/77, 9%) suggested mucosal injury even in the patients without gastrointestinal symptoms. HSP was often preceded by various bacterial, especially streptococcal (36%) and viral infections. Previous streptococcal infection did not induce changes in the level of complement component C3. Recurrences were more frequent in patients >8 years of age (OR 3.7, CI 2.0 to 7.0, p<0.001) and in patients with nephritis (OR 4.6, CI 2.3 to 8.9, p<0.001). Patients with severe HSP nephritis had more extrarenal symptoms up to 6 months. There was no difference in the clinical course between the prednisone-treated and non-treated patients during the 6-month follow-up. Conclusions Serum albumin is often low in HSP patients without proteinuria, due to protein loss via the intestine. Although corticosteroids alleviate the symptoms, they seem not to alter the clinical course of HSP during 6 months of follow-up. [ABSTRACT FROM AUTHOR]
- Published
- 2010
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34. Adequacy of dialysis with tidal and continuous cycling peritoneal dialysis in children.
- Author
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Hölttä, T, Rönnholm, K, and Holmberg, C
- Abstract
Today the major outcome measure for peritoneal dialysis is adequacy. We seek the optimal dialysis modality and prescription for each patient. Tidal dialysis (TPD) was introduced in 1990 to increase efficacy. However, studies with TPD have been inconsistent, and results in small children are lacking.
- Published
- 2000
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35. Finnish centre of excellence in physics, chemistry, biology and meteorology of atmospheric composition and climate change: Summary and outlook
- Author
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Kulmala, M., Lappalainen, H. K., Bäck, J., Timo Vesala, Boy, M., Ehn, M., Hämeri, K., Hölttä, T., Junninen, H., Järvi, L., Kurten, T., Lauri, A., Lehtipalo, K., Mammarella, I., Manninen, H. E., Petäjä, T., Pihlatie, M., Rinne, J., Ruuskanen, T., Sipilä, M., Sorvari, S., Vehkamäki, H., Worsnop, D. R., Kerminen, V. -M, Laaksonen, A., Viisanen, Y., Aalto, T., Hakola, H., Laurila, T., Lihavainen, H., Nikinmaa, E., Hari, P., Lintunen, A., Pumpanen, J., Romakkaniemi, S., Virtanen, A., Riekkola, M. -L, Hartonen, K., and Dal Maso, M.
36. Finnish centre of excellence in physics, chemistry, biology and meteorology of atmospheric composition and climate change: Summary and outlook
- Author
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Kulmala, M., Lappalainen, H. K., Bäck, J., Vesala, T., Boy, M., Ehn, M., Hämeri, K., Hölttä, T., Junninen, H., Järvi, L., Kurten, T., Lauri, A., Lehtipalo, K., Mammarella, I., Manninen, H. E., Petäjä, T., Pihlatie, M., Rinne, J., Ruuskanen, T., Sipilä, M., Sorvari, S., Vehkamäki, H., Worsnop, D. R., Kerminen, V. -M, Laaksonen, A., Viisanen, Y., Aalto, T., Hakola, H., Laurila, T., Lihavainen, H., Eero Nikinmaa, Hari, P., Lintunen, A., Pumpanen, J., Romakkaniemi, S., Virtanen, A., Riekkola, M. -L, Hartonen, K., and Dal Maso, M.
37. Drought effects on carbon allocation to resin defences and on resin dynamics in old-grown Scots pine
- Author
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Rissanen, K., Hölttä, T., Bäck, J., Rigling, A., Wermelinger, B., and Gessler, A.
- Subjects
stomatognathic system ,Drought ,fungi ,Scots pine ,food and beverages ,Carbon allocation ,15. Life on land ,Irrigation ,Resin ,Tree defence - Abstract
Droughts and other rapid changes in abiotic environmental conditions can predispose trees to damage by pest insects and pathogens. For survival of coniferous trees, functional resin-based defences are essential, and it is important to know how they react to changes in environmental conditions at various time scales. We studied the effects of differing water availabilities on resin-based defences in mature Scots pine (Pinus sylvestris) trees in a naturally drought-prone forest within a long-term irrigation experiment. Our objectives were to understand the effects of long-term drought on carbon allocation to resin production and to analyse its influence on resin flow and pressure in comparison to the shorter-term effects of seasonal drought. We tracked carbon allocation to resin after 13C-pulse labelling experiment in late summer 2017 and compared the observed resin dynamics between drought-exposed control trees and irrigated trees from June to August during the dry hot summer of 2018. Dry control trees showed higher allocation of labelled carbon to resin than irrigated trees. Resin pressure was higher in dry control than in irrigated trees with similar water potentials, and resin flow in June was higher in dry control than in irrigated trees with similar crown transparency. Yet, resin pressures of dry control trees in particular decreased with decreasing water availability from June to August. Resin flow was little affected by short-term changes in water availability and mostly associated with crown transparency. We suggest that because of differing timescales of direct drought effects and changes in allocation patterns, dry conditions may support resin-based defences in the long term, but a drought period decreases resin pressure in the short term. © 2021 The Author(s), Environmental and Experimental Botany, 185, ISSN:0098-8472, ISSN:1873-7307
38. Finnish centre of excellence in physics, chemistry, biology and meteorology of atmospheric composition and climate change: Summary and outlook
- Author
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Kulmala, M., Lappalainen, H. K., Bäck, J., Vesala, T., Boy, M., Ehn, M., Hämeri, K., Hölttä, T., Junninen, H., Järvi, L., Kurten, T., Lauri, A., Lehtipalo, K., Mammarella, I., Manninen, H. E., Petäjä, T., Pihlatie, M., Rinne, J., Ruuskanen, T., Sipilä, M., Sorvari, S., Vehkamäki, H., Worsnop, D. R., Kerminen, V. -M, Laaksonen, A., Viisanen, Y., Aalto, T., Laurila, T., Lihavainen, H., Nikinmaa, E., Hari, P., Lintunen, A., Pumpanen, J., Sami Romakkaniemi, Virtanen, A., Riekkola, M. -L, Hartonen, K., and Dal Maso, M.
39. Determination of thermal expansion of green wood and the accuracy of tree stem diameter variation measurements
- Author
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Sevanto, S., Hölttä, T., Hirsikko, A., Timo Vesala, and Nikinmaa, E.
40. Estimation of steady water flux density in a porous medium by Fourier analysis of temperature variations in a cyclic heat pulse system
- Author
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E.F. Sousa, Frédéric Do, M.A. Santolin, Universidade Estadual do Norte Fluminense Darcy Ribeiro (UENF), Universidade Federal do Espirito Santo (UFES), Ecologie fonctionnelle et biogéochimie des sols et des agro-écosystèmes (UMR Eco&Sols), Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad)-Institut de Recherche pour le Développement (IRD)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro), Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), Hölttä, T. (ed.), and Salmon, Y. (ed.)
- Subjects
0106 biological sciences ,Convection ,0303 health sciences ,Materials science ,[SDV]Life Sciences [q-bio] ,Mechanics ,Horticulture ,Thermal diffusivity ,01 natural sciences ,03 medical and health sciences ,symbols.namesake ,Pressure head ,Amplitude ,[MATH.MATH-GM]Mathematics [math]/General Mathematics [math.GM] ,Fourier analysis ,Thermocouple ,Phase (matter) ,symbols ,[SDV.BV]Life Sciences [q-bio]/Vegetal Biology ,Porous medium ,030304 developmental biology ,010606 plant biology & botany - Abstract
We tested a novel theoretical model that determines the steady water flux density in a porous medium from Fourier analysis of temperature variations induced by a cyclic heat pulse system. The model depends on the thermal diffusivity of the medium and on the relative spatial variation of the amplitude and phase of the first order sinusoidal component of the heat wave. The model was tested by using a hydraulic column made of a PVC pipe filled with sawdust. The sensor consisted of two hypodermic needles spaced 7 mm apart. One needle contained a heater and a thermocouple while the other contained only a thermocouple. Different combinations of heating and cooling cycles were tested. The flow was controlled by pressure head and volumetrically measured at the outlet of the tube. The experimental results supported the theoretical model. In particular, the convective index defined in terms of the variations of amplitude and phase of the first component of the heat wave was linearly related to the measured flux density, as predicted. The model was independent of the different combinations of heating and cooling cycles. The estimated water flux density was strongly related to the measured flux density (R2>0.99), having the same slope for the different combinations. The first results of this new approach of cyclic heat pulse system are very promising and suggest further studies and field applications.
- Published
- 2019
41. A Coupled Model of Hydraulic Eco-Physiology and Cambial Growth - Accounting for Biophysical Limitations and Phenology Improves Stem Diameter Prediction at High Temporal Resolution.
- Author
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Liu C, Peltoniemi M, Alekseychik P, Mäkelä A, and Hölttä T
- Abstract
Traditional photosynthesis-driven growth models have considerable uncertainties in predicting tree growth under changing climates, partially because sink activities are directly affected by the environment but not adequately addressed in growth modelling. Therefore, we developed a semi-mechanistic model coupling stomatal optimality, temperature control of enzymatic activities and phenology of cambial growth. Parameterized using Bayesian inference and measured data on Picea abies and Pinus sylvestris in peatland and mineral soils in Finland, the coupled model simulates transpiration and assimilation rates and stem radial dimension (SRD) simultaneously at 30 min resolution. The results suggest that both the sink and phenological formulations with environmental effects are indispensable for capturing SRD dynamics across hourly to seasonal scales. Simulated using the model, growth was more sensitive than assimilation to temperature and soil water, suggesting carbon gain is not driving growth at the current temporal scale. Also, leaf-specific production was occasionally positively correlated with growth duration but not with growth onset timing or annual cambial area increment. Thus, as it is hardly explained by carbon gain, phenology itself should be included in sink-driven growth models of the trees in the boreal zone and possibly other environments where sink activities and photosynthesis are both restrained by harsh conditions., (© 2024 The Author(s). Plant, Cell & Environment published by John Wiley & Sons Ltd.)
- Published
- 2024
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42. Partitioning seasonal stem carbon dioxide efflux into stem respiration, bark photosynthesis, and transport-related flux in Scots pine.
- Author
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Dukat P, Hölttä T, Oren R, Salmon Y, Urbaniak M, Vesala T, Aalto J, and Lintunen A
- Subjects
- Biological Transport, Xylem metabolism, Xylem physiology, Carbon Dioxide metabolism, Photosynthesis physiology, Pinus sylvestris metabolism, Pinus sylvestris physiology, Pinus sylvestris growth & development, Seasons, Plant Stems metabolism, Plant Stems physiology, Plant Stems growth & development, Plant Bark metabolism, Plant Bark physiology, Cell Respiration
- Abstract
Stem CO2 efflux is an important component of the carbon balance in forests. The efflux is considered to principally reflect the net result of two dominating and opposing processes: stem respiration and stem photosynthesis. In addition, transport of CO2 in xylem sap is thought to play an appreciable role in affecting the net flux. This work presents an approach to partition stem CO2 efflux among these processes using sap-flux data and CO2-exchange measurements from dark and transparent chambers placed on mature Scots pine (Pinus sylvestris) trees. Seasonal changes and monthly parameters describing the studied processes were determined. Respiration contributed most to stem net CO2 flux, reaching up to 79% (considering the sum of the absolute values of stem respiration, stem photosynthesis, and flux from CO2 transported in xylem sap to be 100%) in June, when stem growth was greatest. The contribution of photosynthesis accounted for up to 13% of the stem net CO2 flux, increasing over the monitoring period. CO2 transported axially with sap flow decreased towards the end of the growing season. At a reference temperature, respiration decreased starting around midsummer, while its temperature sensitivity increased during the summer. A decline was observed for photosynthetic quantum yield around midsummer together with a decrease in light-saturation point. The proposed approach facilitates modeling net stem CO2 flux at a range of time scales., (© The Author(s) 2024. Published by Oxford University Press on behalf of the Society for Experimental Biology.)
- Published
- 2024
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43. Seasonal dynamics and punctuated carbon sink reduction suggest photosynthetic capacity of boreal silver birch is reduced by the accumulation of hexose.
- Author
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Tian M, Salmon Y, Lintunen A, Oren R, and Hölttä T
- Subjects
- Carbon Sequestration, Water metabolism, Nitrogen metabolism, Carbon metabolism, Starch metabolism, Photosynthesis physiology, Plant Leaves physiology, Plant Leaves metabolism, Betula physiology, Betula metabolism, Seasons, Hexoses metabolism
- Abstract
The 'assimilates inhibition hypothesis' posits that accumulation of nonstructural carbohydrates (NSCs) in leaves reduces leaf net photosynthetic rate, thus internally regulating photosynthesis. Experimental work provides equivocal support mostly under controlled conditions without identifying a particular NSC as involved in the regulation. We combined 3-yr in situ leaf gas exchange observations (natural dynamics) in the upper crown of mature Betula pendula simultaneously with measurements of concentrations of sucrose, hexoses (glucose and fructose), and starch, and similar measurements during several one-day shoot girdling (perturbation dynamics). Leaf water potential and water and nitrogen content were measured to account for their possible contribution to photosynthesis regulation. Leaf photosynthetic capacity (A/C
i ) was temporally negatively correlated with NSC accumulation under both natural and perturbation states. For developed leaves, leaf hexose concentration explained A/Ci variation better than environmental variables (temperature history and daylength); the opposite was observed for developing leaves. The weaker correlations between NSCs and A/Ci in developing leaves may reflect their strong internal sink strength for carbohydrates. By contrast, the strong decline in photosynthetic capacity with NSCs accumulation in mature leaves, observed most clearly with hexose, and even more tightly with its constituents, provides support for the role of assimilates in regulating photosynthesis under natural conditions., (© 2024 The Authors. New Phytologist © 2024 New Phytologist Foundation.)- Published
- 2024
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- View/download PDF
44. Late nephrectomy in infants with congenital nephrotic syndrome of the Finnish type.
- Author
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Suihko A, Tainio J, Tuokkola J, Ylinen E, Hölttä T, and Jahnukainen T
- Subjects
- Humans, Male, Female, Infant, Retrospective Studies, Time Factors, Infant, Newborn, Finland, Nephrectomy methods, Nephrectomy adverse effects, Nephrotic Syndrome surgery, Nephrotic Syndrome complications, Kidney Transplantation
- Abstract
Aim: Bilateral nephrectomy is commonly performed in patients with congenital nephrotic syndrome of the Finnish type. The optimal timing of nephrectomy is unclear., Methods: Growth, thromboembolic events, infections, transplant-related complications and ability to eat were compared between infants with early (Group 1, n = 13) and late (Group 2, n = 10) nephrectomy. 'Early' was defined as nephrectomy at 7-kg body weight followed by peritoneal dialysis and 'late' as nephrectomy at ≥10 kg followed by 3-4 weeks of haemodialysis and kidney transplantation. Patients were followed until the end of the first post-transplant year., Results: Dialysis time was significantly longer in group 1 than in group 2. Late nephrectomy did not increase the risk for thromboembolic events or septicaemia but decreased tube feeding dependency (group 1 69% vs. group 2 20%, p = 0.019). Motor development at transplantation was considered normal in 80% of the infants with late nephrectomy compared to 31% in the early nephrectomy group (p = 0.019); however, the difference between the groups disappeared by the end of the follow-up., Conclusion: Infants with late nephrectomy have comparative outcome but less feeding tube dependency and better motor development during the first post-transplant months compared to infants with early nephrectomy., (© 2024 The Author(s). Acta Paediatrica published by John Wiley & Sons Ltd on behalf of Foundation Acta Paediatrica.)
- Published
- 2024
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45. Serological responses to immunization during nephrosis in infants with congenital nephrotic syndrome of the Finnish type.
- Author
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Savonius O, Kaskinen A, Hölttä T, Ylinen E, Tainio J, Nieminen T, and Jahnukainen T
- Abstract
Background: Pretransplant vaccination is generally recommended to solid organ transplant recipients. In infants with congenital nephrotic syndrome (CNS), the immune response is hypothetically inferior to other patients due to young age and urinary loss of immunoglobulins, but data on the immunization response in severely nephrotic children remain scarce. If effective, however, early immunization of infants with CNS would clinically be advantageous., Methods: We investigated serological vaccine responses in seven children with CNS who were immunized during nephrosis. Antibody responses to measles-mumps-rubella -vaccine (MMR), a pentavalent DTaP-IPV-Hib -vaccine (diphtheria, tetanus, acellular pertussis, inactivated poliovirus, Haemophilus influenzae type b), varicella vaccine, combined hepatitis A and B vaccine, and pneumococcal conjugate vaccine (PCV) were measured after nephrectomy either before or after kidney transplantation., Results: Immunizations were started at a median age of 7 months [interquartile range (IQR) 7-8], with a concurrent median proteinuria of 36,500 mg/L (IQR 30,900-64,250). Bilateral nephrectomy was performed at a median age of 20 months (IQR 14-25), and kidney transplantation 10-88 days after the nephrectomy. Antibody levels were measured at median 18 months (IQR 6-23) after immunization. Protective antibody levels were detected in all examined children for hepatitis B (5/5), Clostridium tetani (7/7), rubella virus (2/2), and mumps virus (1/1); in 5/6 children for varicella; in 4/6 for poliovirus and vaccine-type pneumococcal serotypes; in 4/7 for Haemophilus influenzae type B and Corynebacterium diphtheriae ; in 1/2 for measles virus; and in 2/5 for hepatitis A. None of the seven children had protective IgG levels against Bordetella pertussis ., Conclusion: Immunization during severe congenital proteinuria resulted in variable serological responses, with both vaccine- and patient-related differences. Nephrosis appears not to be a barrier to successful immunization., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (© 2024 Savonius, Kaskinen, Hölttä, Ylinen, Tainio, Nieminen and Jahnukainen.)
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- 2024
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46. Model of methane transport in tree stems: Case study of sap flow and radial diffusion.
- Author
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Anttila J, Tikkasalo OP, Hölttä T, Lintunen A, Vainio E, Leppä K, Haikarainen IP, Koivula H, Ghasemi Falk H, Kohl L, Launiainen S, and Pihlatie M
- Subjects
- Forests, Betula, Trees, Methane
- Abstract
The transport processes of methane (CH
4 ) in tree stems remain largely unknown, although they are critical in assessing the whole-forest CH4 dynamics. We used a physically based dynamic model to study the spatial and diurnal dynamics of stem CH4 transport and fluxes. We parameterised the model using data from laboratory experiments with Pinus sylvestris and Betula pendula and compared the model to experimental data from a field study. Stem CH4 flux in laboratory and field conditions were explained by the axial advective CH4 transport from soil with xylem sap flow and the radial CH4 diffusion through the stem conditions. Diffusion resistance caused by the bark permeability did not significantly affect gas transport or stem CH4 flux in the laboratory experiments. The role of axial diffusion of CH4 in trees was unresolved and requires further studies. Due to the transit time of CH4 in the stem, the diurnal dynamics of stem CH4 fluxes can deviate markedly from the diurnal dynamics of sap flow., (© 2023 The Authors. Plant, Cell & Environment published by John Wiley & Sons Ltd.)- Published
- 2024
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47. Axial conduit widening, tree height, and height growth rate set the hydraulic transition of sapwood into heartwood.
- Author
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Petit G, Mencuccini M, Carrer M, Prendin AL, and Hölttä T
- Subjects
- Plant Leaves, Water, Trees, Xylem
- Abstract
The size-related xylem adjustments required to maintain a constant leaf-specific sapwood conductance (KLEAF) with increasing height (H) are still under discussion. Alternative hypotheses are that: (i) the conduit hydraulic diameter (Dh) at any position in the stem and/or (ii) the number of sapwood rings at stem base (NSWr) increase with H. In addition, (iii) reduced stem elongation (ΔH) increases the tip-to-base conductance through inner xylem rings, thus possibly the NSWr contributing to KLEAF. A detailed stem analysis showed that Dh increased with the distance from the ring apex (DCA) in all rings of a Picea abies and a Fagus sylvatica tree. Net of DCA effect, Dh did not increase with H. Using sapwood traits from a global dataset, NSWr increased with H, decreased with ΔH, and the mean sapwood ring width (SWrw) increased with ΔH. A numerical model based on anatomical patterns predicted the effects of H and ΔH on the conductance of inner xylem rings. Our results suggest that the sapwood/heartwood transition depends on both H and ΔH, and is set when the carbon allocation to maintenance respiration of living cells in inner sapwood rings produces a lower gain in total conductance than investing the same carbon in new vascular conduits., (© The Author(s) 2023. Published by Oxford University Press on behalf of the Society for Experimental Biology. All rights reserved. For permissions, please email: journals.permissions@oup.com.)
- Published
- 2023
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48. Drivers of intra-seasonal δ 13 C signal in tree-rings of Pinus sylvestris as indicated by compound-specific and laser ablation isotope analysis.
- Author
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Rinne-Garmston KT, Tang Y, Sahlstedt E, Adamczyk B, Saurer M, Salmon Y, Carrasco MDRD, Hölttä T, Lehmann MM, Mo L, and Young GHF
- Subjects
- Trees metabolism, Seasons, Carbon Isotopes analysis, Carbohydrates analysis, Plant Leaves metabolism, Sucrose metabolism, Pinus sylvestris metabolism, Laser Therapy, Pinus metabolism
- Abstract
Carbon isotope composition of tree-ring (δ
13 CRing ) is a commonly used proxy for environmental change and ecophysiology. δ13 CRing reconstructions are based on a solid knowledge of isotope fractionations during formation of primary photosynthates (δ13 CP ), such as sucrose. However, δ13 CRing is not merely a record of δ13 CP . Isotope fractionation processes, which are not yet fully understood, modify δ13 CP during sucrose transport. We traced, how the environmental intra-seasonal δ13 CP signal changes from leaves to phloem, tree-ring and roots, for 7 year old Pinus sylvestris, using δ13 C analysis of individual carbohydrates, δ13 CRing laser ablation, leaf gas exchange and enzyme activity measurements. The intra-seasonal δ13 CP dynamics was clearly reflected by δ13 CRing , suggesting negligible impact of reserve use on δ13 CRing . However, δ13 CP became increasingly13 C-enriched during down-stem transport, probably due to post-photosynthetic fractionations such as sink organ catabolism. In contrast, δ13 C of water-soluble carbohydrates, analysed for the same extracts, did not reflect the same isotope dynamics and fractionations as δ13 CP , but recorded intra-seasonal δ13 CP variability. The impact of environmental signals on δ13 CRing , and the 0.5 and 1.7‰ depletion in photosynthates compared ring organic matter and tree-ring cellulose, respectively, are useful pieces of information for studies exploiting δ13 CRing ., (© 2023 The Authors. Plant, Cell & Environment published by John Wiley & Sons Ltd.)- Published
- 2023
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49. A model bridging waterlogging, stomatal behavior and water use in trees in drained peatland.
- Author
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Liu C, Wang Q, Mäkelä A, Hökkä H, Peltoniemi M, and Hölttä T
- Subjects
- Plant Leaves, Plant Stomata, Plant Transpiration, Soil, Pinus sylvestris, Trees
- Abstract
Waterlogging causes hypoxic or anoxic conditions in soils, which lead to decreases in root and stomatal hydraulic conductance. Although these effects have been observed in a variety of plant species, they have not been quantified continuously over a range of water table depths (WTD) or soil water contents (SWC). To provide a quantitative theoretical framework for tackling this issue, we hypothesized similar mathematical descriptions of waterlogging and drought effects on whole-tree hydraulics and constructed a hierarchical model by connecting optimal stomata and soil-to-leaf hydraulic conductance models. In the model, the soil-to-root conductance is non-monotonic with WTD to reflect both the limitations by water under low SWC and by hypoxic effects associated with inhibited oxygen diffusion under high SWC. The model was parameterized using priors from literature and data collected over four growing seasons from Scots pine (Pinus sylvestris L.) trees grown in a drained peatland in Finland. Two reference models (RMs) were compared with the new model, RM1 with no belowground hydraulics and RM2 with no waterlogging effects. The new model was more accurate than the RMs in predicting transpiration rate (fitted slope of measured against modeled transpiration rate = 0.991 vs 0.979 (RM1) and 0.984 (RM2), R2 = 0.801 vs 0.665 (RM1) and 0.776 (RM2)). Particularly, RM2's overestimation of transpiration rate under shallow water table conditions (fitted slope = 0.908, R2 = 0.697) was considerably reduced by the new model (fitted slope = 0.956, R2 = 0.711). The limits and potential improvements of the model are discussed., (© The Author(s) 2022. Published by Oxford University Press.)
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- 2022
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50. The importance of tree internal water storage under drought conditions.
- Author
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Preisler Y, Hölttä T, Grünzweig JM, Oz I, Tatarinov F, Ruehr NK, Rotenberg E, and Yakir D
- Subjects
- Ecosystem, Forests, Plant Transpiration, Water, Droughts, Trees
- Abstract
Global warming and drying trends, as well as the increase in frequency and intensity of droughts, may have unprecedented impacts on various forest ecosystems. We assessed the role of internal water storage (WS) in drought resistance of mature pine trees in the semi-arid Yatir Forest. Transpiration (T), soil moisture and sap flow (SF) were measured continuously, accompanied by periodical measurements of leaf and branch water potential (Ψleaf) and water content (WC). The data were used to parameterize a tree hydraulics model to examine the impact of WS capacitance on the tree water relations. The results of the continuous measurements showed a 5-h time lag between T and SF in the dry season, which peaked in the early morning and early afternoon, respectively. A good fit between model results and observations was only obtained when the empirically estimated WS capacitance was included in the model. Without WS during the dry season, Ψleaf would drop below a threshold known to cause hydraulic failure and cessation of gas exchange in the studied tree species. Our results indicate that tree WS capacitance is a key drought resistance trait that could enhance tree survival in a drying climate, contributing up to 45% of the total daily transpiration during the dry season., (© The Author(s) 2021. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.)
- Published
- 2022
- Full Text
- View/download PDF
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