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Abstract The soil moisture regime may affect dormancy of seeds and their sensitivity to signals that promote germination. We studied the effect of moisture regime on the sensitivity to light of dormant Bromus catharticus seeds, and on the emergence pattern of seedlings. Seeds were incubated under continuously hydrated, continuously dehydrated, or fluctuating moisture regimes in a controlled environment (258C, darkness) for 2 months. After moisture treatments, seeds were exposed to red or far-red light pulses, or to darkness, to determine germinability. In addition, grassland mesocosms with intact seed bank and vegetation were irrigated or subjected to a drought regime in a glasshouse at summer temperatures. After 2 months, the temperature was reduced to correspond to grassland temperatures in autumn; the canopy was removed and half of the mesocosms were covered with filters that exclude red light. Density of B. catharticus darkness) for 2 months. After moisture treatments, seeds were exposed to red or far-red light pulses, or to darkness, to determine germinability. In addition, grassland mesocosms with intact seed bank and vegetation were irrigated or subjected to a drought regime in a glasshouse at summer temperatures. After 2 months, the temperature was reduced to correspond to grassland temperatures in autumn; the canopy was removed and half of the mesocosms were covered with filters that exclude red light. Density of B. catharticus seedlings. Seeds were incubated under continuously hydrated, continuously dehydrated, or fluctuating moisture regimes in a controlled environment (258C, darkness) for 2 months. After moisture treatments, seeds were exposed to red or far-red light pulses, or to darkness, to determine germinability. In addition, grassland mesocosms with intact seed bank and vegetation were irrigated or subjected to a drought regime in a glasshouse at summer temperatures. After 2 months, the temperature was reduced to correspond to grassland temperatures in autumn; the canopy was removed and half of the mesocosms were covered with filters that exclude red light. Density of B. catharticus darkness) for 2 months. After moisture treatments, seeds were exposed to red or far-red light pulses, or to darkness, to determine germinability. In addition, grassland mesocosms with intact seed bank and vegetation were irrigated or subjected to a drought regime in a glasshouse at summer temperatures. After 2 months, the temperature was reduced to correspond to grassland temperatures in autumn; the canopy was removed and half of the mesocosms were covered with filters that exclude red light. Density of B. catharticus catharticus seeds, and on the emergence pattern of seedlings. Seeds were incubated under continuously hydrated, continuously dehydrated, or fluctuating moisture regimes in a controlled environment (258C, darkness) for 2 months. After moisture treatments, seeds were exposed to red or far-red light pulses, or to darkness, to determine germinability. In addition, grassland mesocosms with intact seed bank and vegetation were irrigated or subjected to a drought regime in a glasshouse at summer temperatures. After 2 months, the temperature was reduced to correspond to grassland temperatures in autumn; the canopy was removed and half of the mesocosms were covered with filters that exclude red light. Density of B. catharticus darkness) for 2 months. After moisture treatments, seeds were exposed to red or far-red light pulses, or to darkness, to determine germinability. In addition, grassland mesocosms with intact seed bank and vegetation were irrigated or subjected to a drought regime in a glasshouse at summer temperatures. After 2 months, the temperature was reduced to correspond to grassland temperatures in autumn; the canopy was removed and half of the mesocosms were covered with filters that exclude red light. Density of B. catharticus seedlings. Seeds were incubated under continuously hydrated, continuously dehydrated, or fluctuating moisture regimes in a controlled environment (258C, darkness) for 2 months. After moisture treatments, seeds were exposed to red or far-red light pulses, or to darkness, to determine germinability. In addition, grassland mesocosms with intact seed bank and vegetation were irrigated or subjected to a drought regime in a glasshouse at summer temperatures. After 2 months, the temperature was reduced to correspond to grassland temperatures in autumn; the canopy was removed and half of the mesocosms were covered with filters that exclude red light. Density of B. catharticus darkness) for 2 months. After moisture treatments, seeds were exposed to red or far-red light pulses, or to darkness, to determine germinability. In addition, grassland mesocosms with intact seed bank and vegetation were irrigated or subjected to a drought regime in a glasshouse at summer temperatures. After 2 months, the temperature was reduced to correspond to grassland temperatures in autumn; the canopy was removed and half of the mesocosms were covered with filters that exclude red light. Density of B. catharticus Bromus catharticus seeds, and on the emergence pattern of seedlings. Seeds were incubated under continuously hydrated, continuously dehydrated, or fluctuating moisture regimes in a controlled environment (258C, darkness) for 2 months. After moisture treatments, seeds were exposed to red or far-red light pulses, or to darkness, to determine germinability. In addition, grassland mesocosms with intact seed bank and vegetation were irrigated or subjected to a drought regime in a glasshouse at summer temperatures. After 2 months, the temperature was reduced to correspond to grassland temperatures in autumn; the canopy was removed and half of the mesocosms were covered with filters that exclude red light. Density of B. catharticus darkness) for 2 months. After moisture treatments, seeds were exposed to red or far-red light pulses, or to darkness, to determine germinability. In addition, grassland mesocosms with intact seed bank and vegetation were irrigated or subjected to a drought regime in a glasshouse at summer temperatures. After 2 months, the temperature was reduced to correspond to grassland temperatures in autumn; the canopy was removed and half of the mesocosms were covered with filters that exclude red light. Density of B. catharticus seedlings. Seeds were incubated under continuously hydrated, continuously dehydrated, or fluctuating moisture regimes in a controlled environment (258C, darkness) for 2 months. After moisture treatments, seeds were exposed to red or far-red light pulses, or to darkness, to determine germinability. In addition, grassland mesocosms with intact seed bank and vegetation were irrigated or subjected to a drought regime in a glasshouse at summer temperatures. After 2 months, the temperature was reduced to correspond to grassland temperatures in autumn; the canopy was removed and half of the mesocosms were covered with filters that exclude red light. Density of B. catharticus darkness) for 2 months. After moisture treatments, seeds were exposed to red or far-red light pulses, or to darkness, to determine germinability. In addition, grassland mesocosms with intact seed bank and vegetation were irrigated or subjected to a drought regime in a glasshouse at summer temperatures. After 2 months, the temperature was reduced to correspond to grassland temperatures in autumn; the canopy was removed and half of the mesocosms were covered with filters that exclude red light. Density of B. catharticus seeds, and on the emergence pattern of seedlings. Seeds were incubated under continuously hydrated, continuously dehydrated, or fluctuating moisture regimes in a controlled environment (258C, darkness) for 2 months. After moisture treatments, seeds were exposed to red or far-red light pulses, or to darkness, to determine germinability. In addition, grassland mesocosms with intact seed bank and vegetation were irrigated or subjected to a drought regime in a glasshouse at summer temperatures. After 2 months, the temperature was reduced to correspond to grassland temperatures in autumn; the canopy was removed and half of the mesocosms were covered with filters that exclude red light. Density of B. catharticus darkness) for 2 months. After moisture treatments, seeds were exposed to red or far-red light pulses, or to darkness, to determine germinability. In addition, grassland mesocosms with intact seed bank and vegetation were irrigated or subjected to a drought regime in a glasshouse at summer temperatures. After 2 months, the temperature was reduced to correspond to grassland temperatures in autumn; the canopy was removed and half of the mesocosms were covered with filters that exclude red light. Density of B. catharticus 8C, darkness) for 2 months. After moisture treatments, seeds were exposed to red or far-red light pulses, or to darkness, to determine germinability. In addition, grassland mesocosms with intact seed bank and vegetation were irrigated or subjected to a drought regime in a glasshouse at summer temperatures. After 2 months, the temperature was reduced to correspond to grassland temperatures in autumn; the canopy was removed and half of the mesocosms were covered with filters that exclude red light. Density of B. catharticusB. catharticus seedlings was evaluated after 2 weeks. Dormancy decreased in continuously hydrated seeds but they still required red light for germination. In contrast, an important fraction of seeds that experienced continuously dehydrated or fluctuating moisture regimes germinated in darkness or after far-red light pulses. In the mesocosms that had experienced a soil drought, a higher density of seedlings emerged in the absence of red light than in the daily irrigated mesocosms. This indicates that a fraction of B. catharticus seeds acquired the capability to germinate under the canopy, especially in the drought moisture regime. Results indicate that the soil moisture environment experienced during dormancy affects the sensitivity to light of B. catharticus seeds, as well as the emergence pattern of seedlings. pattern of seedlings. acquired the capability to germinate under the canopy, especially in the drought moisture regime. Results indicate that the soil moisture environment experienced during dormancy affects the sensitivity to light of B. catharticus seeds, as well as the emergence pattern of seedlings. pattern of seedlings. B. catharticus seeds acquired the capability to germinate under the canopy, especially in the drought moisture regime. Results indicate that the soil moisture environment experienced during dormancy affects the sensitivity to light of B. catharticus seeds, as well as the emergence pattern of seedlings. pattern of seedlings. B. catharticus seeds, as well as the emergence pattern of seedlings.